DISEASES

Disease-gene associations mined from literature

Human genes for osteochondrodysplasia

Osteochondrodysplasia [DOID:2256]

A bone development disease that results_in defective development of located_in cartilage or located_in bone.

Synonyms:  osteochondrodysplasia,  DOID:2256,  Cartilage Development disorder,  Congenital anomaly of cartilage (disorder),  Osteochondrodysplasia syndrome (disorder) ...